| Issue Date |
Title |
Author(s) |
| 2015 |
Amplicon Resequencing Identified Parental Mosaicism for Approximately 10% of "de novo" SCN1A Mutations in Children with Dravet Syndrome |
Xu, Xiaojing;Yang, Xiaoxu;Wu, Qixi;Liu, Aijie;Yang, Xiaoling;Ye, Adam Yongxin;Huang, August Yue;Li, Jiarui;Wang, Meng;Yu, Zhe;Wang, Sheng;Zhang, Zhichao;Wu, Xiru;Wei, Liping;Zhang, Yuehua |
| 2019 |
ATP1A3 mosaicism in families with alternating hemiplegia of childhood |
Yang, Xiaoling;Yang, Xiaoxu;Chen, Jiaoyang;Li, Shupin;Zeng, Qi;Huang, August Y.;Ye, Adam Y.;Yu, Zhe;Wang, Sheng;Jiang, Yuwu;Wu, Xiru;Wu, Qixi;Wei, Liping;Zhang, Yuehua |
| 2018 |
AutismKB 2.0: a knowledgebase for the genetic evidence of autism spectrum disorder |
Yang, Changhong;Li, Jiarui;Wu, Qixi;Yang, Xiaoxu;Huang, August Yue;Zhang, Jie;Ye, Adam Yongxin;Dou, Yanmei;Yan, Linlin;Zhou, Wei-zhen;Kong, Lei;Wang, Meng;Ai, Chen;Yang, Dechang;Wei, Liping |
| Dec-2022 |
Detecting genomic mosaicism in "de novo" genetic epilepsy by amplicon-based deep sequencing |
Chen, Jiaoyang;Chen, Yi;Yang, Ying;Niu, Xueyang;Zhang, Jing;Zeng, Qi;Liu, Aijie;Xu, Xiaojing;Yang, Xiaoxu;Li, Shupin;Yang, Xiaoling;Wang, Yi;Zhang, Yuehua |
| 2017 |
Genomic mosaicism in paternal sperm and multiple parental tissues in a Dravet syndrome cohort |
Yang, Xiaoxu;Liu, Aijie;Xu, Xiaojing;Yang, Xiaoling;Zeng, Qi;Ye, Adam Yongxin;Yu, Zhe;Wang, Sheng;Huang, August Yue;Wu, Xiru;Wu, Qixi;Wei, Liping;Zhang, Yuehua |
| 2019 |
Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort |
Zhang, Qingping;Yang, Xiaoxu;Wang, Jiaping;Li, Jiarui;Wu, Qixi;Wen, Yongxin;Zhao, Ying;Zhang, Xiaoying;Yao, He;Wu, Xiru;Yu, Shujie;Wei, Liping;Bao, Xinhua |
| 2019 |
Genomic mosaicism in the pathogenesis and inheritance of a Rett syndrome cohort (vol 21, pg 1330, 2019) |
Zhang, Qingping;Yang, Xiaoxu;Wang, Jiaping;Li, Jiarui;Wu, Qixi;Wen, Yongxin;Zhao, Ying;Zhang, Xiaoying;Yao, He;Wu, Xiru;Yu, Shujie;Wei, Liping;Bao, Xinhua |
| 2017 |
MosaicHunter: accurate detection of postzygotic single-nucleotide mosaicism through next-generation sequencing of unpaired, trio, and paired samples |
Huang, August Yue;Zhang, Zheng;Ye, Adam Yongxin;Dou, Yanmei;Yan, Linlin;Yang, Xiaoxu;Zhang, Yuehua;Wei, Liping |
| 2019 |
Mosaicism and incomplete penetrance of PCDH19 mutations |
Liu, Aijie;Yang, Xiaoxu;Yang, Xiaoling;Wu, Qixi;Zhang, Jing;Sun, Dan;Yang, Zhixian;Jiang, Yuwu;Wu, Xiru;Wei, Liping;Zhang, Yuehua |
| 3-Nov-2022 |
PCDH19-related epilepsy in mosaic males: The phenotypic implication of genotype and variant allele frequency |
Chen, Yi;Yang, Xiaoxu;Chen, Jiaoyang;Yang, Xiaoling;Yang, Ying;Liu, Aijie;Zhang, Xiaoli;Wu, Wenjuan;Sun, Dan;Yang, Zhixian;Jiang, Yuwu;Zhang, Yuehua |
| 2017 |
Postzygotic single-nucleotide mosaicisms contribute to the etiology of autism spectrum disorder and autistic traits and the origin of mutations |
Dou, Yanmei;Yang, Xiaoxu;Li, Ziyi;Wang, Sheng;Zhang, Zheng;Ye, Adam Yongxin;Yan, Linlin;Yang, Changhong;Wu, Qixi;Li, Jiarui;Zhao, Boxun;Huang, August Yue;Wei, Liping |
| 2014 |
Postzygotic single-nucleotide mosaicisms in whole-genome sequences of clinically unremarkable individuals |
Huang, August Y.;Xu, Xiaojing;Ye, Adam Y.;Wu, Qixi;Yan, Linlin;Zhao, Boxun;Yang, Xiaoxu;He, Yao;Wang, Sheng;Zhang, Zheng;Gu, Bowen;Zhao, Han-Qing;Wang, Meng;Gao, Hua;Gao, Ge;Zhang, Zhichao;Yang, Xiaoling;Wu, Xiru;Zhang, Yuehua;Wei, Liping |
| 2009 |
Proteome analysis of a single zebrafish embryo using three different digestion strategies coupled with liquid chromatography-tandem mass spectrometry |
Lin, Ying;Chen, Yan;Yang, Xiaoxu;Xu, Dong;Liang, Songping |
| 2014 |
"Bioinformatics: Introduction and Methods," a Bilingual Massive Open Online Course (MOOC) as a New Example for Global Bioinformatics Education |
Ding, Yang;Wang, Meng;He, Yao;Ye, Adam Yongxin;Yang, Xiaoxu;Liu, Fenglin;Meng, Yuqi;Gao, Ge;Wei, Liping |
| 2019 |
Somatic LINE-1 retrotransposition in cortical neurons and non-brain tissues of Rett patients and healthy individuals |
Zhao, Boxun;Wu, Qixi;Ye, Adam Yongxin;Guo, Jing;Zheng, Xianing;Yang, Xiaoxu;Yan, Linlin;Liu, Qing-Rong;Hyde, Thomas M.;Wei, Liping;Huang, August Yue |
| 2017 |
Ultrasensitive and high-efficiency screen of de novo low-frequency mutations by o2n-seq |
Wang, Kaile;Lai, Shujuan;Yang, Xiaoxu;Zhu, Tianqi;Lu, Xuemei;Wu, Chung-I;Ruan, Jue |
